A Study to Evaluate the Long-Term Safety and Efficacy of Povorcitinib in Participants With Moderate to Severe Hidradenitis Suppurativa
Condition(s) studied
Study summary
The purpose of this study is to evaluate long-term safety and efficacy of povorcitinib in participants with moderate to severe hidradenitis suppurativa who completed the 54 weeks of study treatment within the originating parent Phase 3 studies (INCB 54707-301 \[NCT05620823\] or INCB 54707-302 \[NCT05620836\]).
Eligibility
Primary outcome measure(s)
- Proportion of participants with Treatment-Emergent Adverse Events (TEAEs) — up to approximately 56 weeks
TEAE is defined as any untoward medical occurrence associated with the use of a drug in humans, whether or not it is considered drug-related. An AE can therefore be any unfavorable or unintended sign (including an abnormal laboratory finding), symptom, or disease (new or exacerbated) temporally associated with the use of study drug.
Trial sites (165)
| Facility | City | Region | Status |
|---|---|---|---|
| Investigative Site US303 | Phoenix | Arizona | |
| Investigative Site US240 | Scottsdale | Arizona | |
| Investigative Site US307 | Fort Smith | Arkansas | |
| Investigative Site US214 | Rogers | Arkansas | |
| Investigative Site US315 | Laguna Niguel | California | |
| Investigative Site US223 | Los Angeles | California | |
| Investigative Site US222 | Oakland | California | |
| Investigative Site US226 | San Diego | California | |
| Investigative Site US309 | Clearwater | Florida | |
| Investigative Site US317 | Hialeah | Florida | |
| Investigative Site US306 | Hollywood | Florida | |
| Investigative Site US320 | Hollywood | Florida | |
| Investigative Site US316 | Maitland | Florida | |
| Investigative Site US227 | Margate | Florida | |
| Investigative Site US204 | Miami | Florida | |
| Investigative Site US236 | Miami | Florida | |
| Investigative Site US321 | North Miami Beach | Florida | |
| Investigative Site US200 | Ocala | Florida | |
| Investigative Site US228 | Tampa | Florida | |
| Investigative Site US201 | Tampa | Florida | |
| Investigative Site US311 | Marietta | Georgia | |
| Investigative Site US220 | West Dundee | Illinois | |
| Investigative Site US206 | Indianapolis | Indiana | |
| Investigative Site US337 | Indianapolis | Indiana | |
| Investigative Site US341 | Bowling Green | Kentucky | |
| Investigative Site US209 | Louisville | Kentucky | |
| Investigative Site US305 | Baton Rouge | Louisiana | |
| Investigative Site US207 | Metairie | Louisiana | |
| Investigative Site US229 | New Orleans | Louisiana | |
| Investigative Site US224 | Baltimore | Maryland | |
| Investigative Site US325 | Marriottsville | Maryland | |
| Investigative Site US225 | Boston | Massachusetts | |
| Investigative Site US304 | Boston | Massachusetts | |
| Investigative Site US310 | Brighton | Massachusetts | |
| Investigative Site US221 | Quincy | Massachusetts | |
| Investigative Site US213 | Fort Gratiot | Michigan | |
| Investigative Site US217 | Waterford | Michigan | |
| Investigative Site US212 | Minneapolis | Minnesota | |
| Investigative Site US302 | St Louis | Missouri | |
| Investigative Site US318 | Portsmouth | New Hampshire |
+ 125 more sites — see the full list on the official registry below.
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Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06212999 on ClinicalTrials.gov ↗ ← All trials in the UK